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豚鼠嗜酸性粒细胞白三烯B4受体的功能特性

Functional properties of guinea pig eosinophil leukotriene B4 receptor.

作者信息

Ng C F, Sun F F, Taylor B M, Wolin M S, Wong P Y

机构信息

Department of Pharmacology, New York Medical College, Valhalla 10595.

出版信息

J Immunol. 1991 Nov 1;147(9):3096-103.

PMID:1655904
Abstract

It is currently thought that pulmonary eosinophils play a proinflammatory role in bronchial asthma. Leukotriene B4 (LTB4) is being considered as an important mediator in regulating eosinophil function because of its potent activities in inducing leukocyte chemotaxis, chemokinesis, degranulation, and aggregation. Because the LTB4 receptor has not been characterized in eosinophils, we report in this study the presence of a functional high affinity receptor for LTB4 on guinea pig (GP) eosinophils. Scatchard analysis of saturation binding studies yielded a Kd of 1.4 +/- 0.2 nM (mean +/- SEM, n = 3) and a Bmax of 1.6 +/- 0.4 pmol/mg of protein for LTB4 in GP eosinophil membranes. A linear Scatchard plot was obtained, suggesting that GP eosinophil membranes expressed only a single high affinity LTB4 receptor population. Saturation binding studies in whole cells also yielded a linear Scatchard plot, with a Kd of 2.8 +/- 0.96 nM (mean +/- SEM, n = 4) and a Bmax of 4 x 10(4) +/- 6 x 10(3) receptors/cell. Competitive binding studies using several compounds with structures similar to that of LTB4 showed that these agents bound to the receptor in the following descending order of affinity (Ki, nM): LTB4 (0.96) less than TB3 (1.0) greater than 20-hydroxy-LTB4 (3.5) greater than 12(R)-hydroxy-5,8,14-cis,10-trans-eicosatetraenoic acid (20) greater than 12(S)-hydroxy-5,8,14-cis,10-trans-eicosatetraenoic acid (231) greater than 20-carboxy-LTB4 (350) greater than 5(S),12(S)-dihydroxy-6,10-trans,8,14-cis-eicosatetraenoic acid (541). This rank order of potency in binding affinity correlates closely with the ability of these compounds to induce both chemotaxis and superoxide anion generation. Analysis of the structure-activity relationship suggests that the 12R-hydroxyl group and a cis double bond at the C-6 position are important for optimal agonist binding to the LTB4 receptor present in GP eosinophil membranes. The results suggest that LTB4 may be an important chemoattractant for eosinophils in GP and may induce the release of reactive oxygen species from this cell.

摘要

目前认为,肺嗜酸性粒细胞在支气管哮喘中发挥促炎作用。白三烯B4(LTB4)因其在诱导白细胞趋化、化学增活、脱颗粒和聚集方面的强大活性,被视为调节嗜酸性粒细胞功能的重要介质。由于LTB4受体在嗜酸性粒细胞中尚未得到表征,我们在本研究中报告了豚鼠(GP)嗜酸性粒细胞上存在功能性LTB4高亲和力受体。对饱和结合研究进行Scatchard分析得出,GP嗜酸性粒细胞膜中LTB4的解离常数(Kd)为1.4±0.2 nM(平均值±标准误,n = 3),最大结合容量(Bmax)为1.6±0.4 pmol/mg蛋白质。获得了线性Scatchard图,表明GP嗜酸性粒细胞膜仅表达单一的高亲和力LTB4受体群体。全细胞中的饱和结合研究也得出了线性Scatchard图,Kd为2.8±0.96 nM(平均值±标准误,n = 4),Bmax为4×10⁴±6×10³个受体/细胞。使用几种结构与LTB4相似的化合物进行的竞争性结合研究表明,这些试剂与受体的结合亲和力顺序如下(抑制常数Ki,nM):LTB4(0.96)<TB3(1.0)>20 - 羟基 - LTB4(3.5)>12(R) - 羟基 - 5,8,14 - 顺式,10 - 反式 - 二十碳四烯酸(20)>12(S) - 羟基 - 5,8,14 - 顺式,10 - 反式 - 二十碳四烯酸(231)>20 - 羧基 - LTB4(350)>5(S),12(S) - 二羟基 - 6,10 - 反式,8,14 - 顺式 - 二十碳四烯酸(541)。这种结合亲和力的效价顺序与这些化合物诱导趋化和超氧阴离子生成的能力密切相关。结构 - 活性关系分析表明,12R - 羟基基团和C - 6位的顺式双键对于最佳激动剂与GP嗜酸性粒细胞膜中存在的LTB4受体结合很重要。结果表明,LTB4可能是GP中嗜酸性粒细胞的重要趋化因子,并可能诱导该细胞释放活性氧。

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